Formic Acid → HCID 19601401, compound
Reaction equation
[OH:1][CH2:2][CH2:3][N:4]1[CH2:8][CH2:7][CH2:6][CH2:5]1.[CH:9](O)=[O:10]>>[CH:9]([O:1][CH2:2][CH2:3][N:4]1[CH2:8][CH2:7][CH2:6][CH2:5]1)=[O:10]Participants
3
Conditions
- Temperature
- 80 °C
Procedure
A mixture of 115 9 of 1-(2-hydroxyethyl)pyrrolidine and 500 g of formic acid was heated at 80° C. for 10 hours. The reaction mixture was concentrated in vacuum, diluted with ethyl acetate, and neutralized with saturated sodium bicarbonate in water. This was followed by separation, water washing, drying over anhydrous sodium sulfate, and vacuum concentration. Purification by vacuum distillation yielded 2-(1-pyrrolidinyl)ethyl formate, designated (B-10].
Workup
- concentrationThe reaction mixture was concentrated in vacuum
- additiondiluted with ethyl acetate
- customThis was followed by separation, water washing
- dry with materialdrying over anhydrous sodium sulfate, and vacuum concentration
- customPurification
- distillationby vacuum distillation
Sources & evidence
- ORD record
- ord-fce5b6ab5e7c4e5281802785328ac31a
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06749988B2
Reaction notes
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